未登录 Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonad Mayere, Chloe; Regard, Violaine; Perea-Gomez, Aitana; Bunce, Corey; Neirijnck, Yasmine; Djari, Cyril; Bellido-Carreras, Natividad; Sararols, Pauline; Reeves, Richard; Greenaway, Simon; Simon, Michelle; Siggers, Pam; Condrea, Diana; Kuhne, Francoise; Gantar, Ivana; Tang, Furong; Stevant, Isabelle; Batti, Laura; Ghyselinck, Norbert B.; Wilhelm, Dagmar; Greenfield, Andy; Capel, Blanche; Chaboissier, Marie-Christine; Nef, Serge 分享 收藏
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes Lana-Elola, Eva; Cater, Heather; Watson-Scales, Sheona; Greenaway, Simon; Mueller-Winkler, Jennifer; Gibbins, Dorota; Nemes, Mihaela; Slender, Amy; Hough, Tertius; Keskivali-Bond, Piia; Scudamore, Cheryl L.; Herbert, Eleanor; Banks, Gareth T.; Mobbs, Helene; Canonica, Tara; Tosh, Justin; Noy, Suzanna; Llorian, Miriam; Nolan, Patrick M.; Griffin, Julian L.; Good, Mark; Simon, Michelle; Mallon, Ann-Marie; Wells, Sara; Fisher, Elizabeth M. C.; Tybulewicz, Victor L. J. 分享 收藏
Linking the FTO obesity rs1421085 variant circuitry to cellular, metabolic, and organismal phenotypes in vivo 将FTO肥胖rs1421085变异电路与体内细胞，代谢和有机体表型联系起来 Laber, Samantha; Forcisi, Sara; Bentley, Liz; Petzold, Julia; Moritz, Franco; Smirnov, Kirill S.; Al Sadat, Loubna; Williamson, Iain; Strobel, Sophie; Agnew, Thomas; Sengupta, Shahana; Nicol, Tom; Grallert, Harald; Heier, Margit; Honecker, Julius; Mianne, Joffrey; Teboul, Lydia; Dumbell, Rebecca; Long, Helen; Simon, Michelle; Lindgren, Cecilia; Bickmore, Wendy A.; Hauner, Hans; Schmitt-Kopplin, Philippe; Claussnitzer, Melina; Cox, Roger D. 分享 收藏
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Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density Swan, Anna L.; Schuett, Christine; Rozman, Jan; Moreno, Maria del Mar Muniz; Brandmaier, Stefan; Simon, Michelle; Leuchtenberger, Stefanie; Griffiths, Mark; Brommage, Robert; Keskivali-Bond, Piia; Grallert, Harald; Werner, Thomas; Teperino, Raffaele; Becker, Lore; Miller, Gregor; Moshiri, Ala; Seavitt, John R.; Cissell, Derek D.; Meehan, Terrence F.; Acar, Elif F.; Lelliott, Christopher J.; Flenniken, Ann M.; Champy, Marie-France; Sorg, Tania; Ayadi, Abdel; Braun, Robert E.; Cater, Heather; Dickinson, Mary E.; Flicek, Paul; Gallegos, Juan; Ghirardello, Elena J.; Heaney, Jason D.; Jacquot, Sylvie; Lally, Connor; Logan, John G.; Teboul, Lydia; Mason, Jeremy; Spielmann, Nadine; McKerlie, Colin; Murray, Stephen A.; Nutter, Lauryl M. J.; Odfalk, Kristian F.; Parkinson, Helen; Prochazka, Jan; Reynolds, Corey L.; Selloum, Mohammed; Spoutil, Frantisek; Svenson, Karen L.; Vales, Taylor S.; Wells, Sara E.; White, Jacqueline K.; Sedlacek, Radislav; Wurst, Wolfgang; Lloyd, Kent K. C.; Croucher, Peter, I; Fuchs, Helmut; Williams, Graham R.; Bassett, Duncan; Gailus-Durner, Valerie; Herault, Yann; Mallon, Ann-Marie; Brown, Steve D. M.; Mayer-Kuckuk, Philipp; de Angelis, Martin Hrabe 分享 收藏
Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13 Livermore, Catherine; Simon, Michelle; Reeves, Richard; Stevant, Isabelle; Nef, Serge; Pope, Madeleine; Mallon, Ann-Marie; Wells, Sara; Warr, Nick; Greenfield, Andy 分享 收藏
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways Agnew, Thomas; Goldsworthy, Michelle; Aguilar, Carlos; Morgan, Anna; Simon, Michelle; Hilton, Helen; Esapa, Chris; Wu, Yixing; Cater, Heather; Bentley, Liz; Scudamore, Cheryl; Poulton, Joanna; Morten, Karl J.; Thompson, Kyle; He, Langping; Brown, Steve D. M.; Taylor, Robert W.; Bowl, Michael R.; Cox, Roger D. 分享 收藏
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease Corrochano, Silvia; Blanco, Gonzalo; Williams, Debbie; Wettstein, Jessica; Simon, Michelle; Kumar, Saumya; Moir, Lee; Agnew, Thomas; Stewart, Michelle; Landman, Allison; Kotiadis, Vassilios N.; Duchen, Michael R.; Wackerhage, Henning; Rubinsztein, David C.; Brown, Steve D. M.; Acevedo-Arozena, Abraham 分享 收藏
Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxiety Moir, Lee; Bochukova, Elena G.; Dumbell, Rebecca; Banks, Gareth; Bains, Rasneer S.; Nolan, Patrick M.; Scudamore, Cheryl; Simon, Michelle; Watson, Kimberly A.; Keogh, Julia; Henning, Elena; Hendricks, Audrey; O'Rahilly, Stephen; Barroso, Ines; Sullivan, Adrienne E.; Bersten, David C.; Whitelaw, Murray L.; Kirsch, Susan; Bentley, Elizabeth; Farooqi, I. Sadaf; Cox, Roger D. 分享 收藏
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The digital revolution in phenotyping 表型的数字革命 Oellrich, Anika; Collier, Nigel; Groza, Tudor; Rebholz-Schuhmann, Dietrich; Shah, Nigam; Bodenreider, Olivier; Boland, Mary Regina; Georgiev, Ivo; Liu, Hongfang; Livingston, Kevin; Luna, Augustin; Mallon, Ann-Marie; Manda, Prashanti; Robinson, Peter N.; Rustici, Gabriella; Simon, Michelle; Wang, Liqin; Winnenburg, Rainer; Dumontier, Michel 分享 收藏
Eye diseases identified in the ENU-Ageing Screen Jackson, I.; Starbuck, B.; McKie, L.; Banks, G.; Blease, A.; Simon, M.; Wisby, L.; Cross, S.; Nolan, P.; Brown, S.; Potter, P. 分享 收藏
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics de Angelis, Martin Hrabe; Nicholson, George; Selloum, Mohammed; White, Jacqueline K.; Morgan, Hugh; Ramirez-Solis, Ramiro; Sorg, Tania; Wells, Sara; Fuchs, Helmut; Fray, Martin; Adams, David J.; Adams, Niels C.; Adler, Thure; Aguilar-Pimentel, Antonio; Ali-Hadji, Dalila; Amann, Gregory; Andre, Philippe; Atkins, Sarah; Auburtin, Aurelie; Ayadi, Abdel; Becker, Julien; Becker, Lore; Bedu, Elodie; Bekeredjian, Raffi; Birling, Marie-Christine; Blake, Andrew; Bottomley, Joanna; Bowl, Michael R.; Brault, Veronique; Busch, Dirk H.; Bussell, James N.; Calzada-Wack, Julia; Cater, Heather; Champy, Marie-France; Charles, Philippe; Chevalier, Claire; Chiani, Francesco; Codner, Gemma F.; Combe, Roy; Cox, Roger; Dalloneau, Emilie; Dierich, Andre; Di Fenza, Armida; Doe, Brendan; Duchon, Arnaud; Eickelberg, Oliver; Esapa, Chris T.; El Fertak, Lahcen; Feigel, Tanja; Emelyanova, Irina; Estabel, Jeanne; Favor, Jack; Flenniken, Ann; Gambadoro, Alessia; Garrett, Lilian; Gates, Hilary; Gerdin, Anna-Karin; Gkoutos, George; Greenaway, Simon; Glasl, Lisa; Goetz, Patrice; Da Cruz, Isabelle Goncalves; Goetz, Alexander; Graw, Jochen; Guimond, Alain; Hans, Wolfgang; Hicks, Geoff; Hoelter, Sabine M.; Hoefler, Heinz; Hancock, John M.; Hoehndorf, Robert; Hough, Tertius; Houghton, Richard; Hurt, Anja; Ivandic, Boris; Jacobs, Hughes; Jacquot, Sylvie; Jones, Nora; Karp, Natasha A.; Katus, Hugo A.; Kitchen, Sharon; Klein-Rodewald, Tanja; Klingenspor, Martin; Klopstock, Thomas; Lalanne, Valerie; Leblanc, Sophie; Lengger, Christoph; le Marchand, Elise; Ludwig, Tonia; Lux, Aline; McKerlie, Colin; Maier, Holger; Mandel, Jean-Louis; Marschall, Susan; Mark, Manuel; Melvin, David G.; Meziane, Hamid; Micklich, Kateryna; Mittelhauser, Christophe; Monassier, Laurent; Moulaert, David; Muller, Stephanie; Naton, Beatrix; Neff, Frauke; Nolan, Patrick M.; Nutter, Lauryl M. J.; Ollert, Markus; Pavlovic, Guillaume; Pellegata, Natalia S.; Peter, Emilie; Petit-Demouliere, Benoit; Pickard, Amanda; Podrini, Christine; Potter, Paul; Pouilly, Laurent; Puk, Oliver; Richardson, David; Rousseau, Stephane; Quintanilla-Fend, Leticia; Quwailid, Mohamed M.; Racz, Ildiko; Rathkolb, Birgit; Riet, Fabrice; Rossant, Janet; Roux, Michel; Rozman, Jan; Ryder, Edward; Salisbury, Jennifer; Santos, Luis; Schaeble, Karl-Heinz; Schiller, Evelyn; Schrewe, Anja; Schulz, Holger; Steinkamp, Ralf; Simon, Michelle; Stewart, Michelle; Stoeger, Claudia; Stoeger, Tobias; Sun, Minxuan; Sunter, David; Teboul, Lydia; Tilly, Isabelle; Tocchini-Valentini, Glauco P.; Tost, Monica; Treise, Irina; Vasseur, Laurent; Velot, Emilie; Vogt-Weisenhorn, Daniela; Wagner, Christelle; Walling, Alison; Wattenhofer-Donze, Marie; Weber, Bruno; Wendling, Olivia; Westerberg, Henrik; Willershaeuser, Monja; Wolf, Eckhard; Wolter, Anne; Wood, Joe; Wurst, Wolfgang; Yildirim, Ali Oender; Zeh, Ramona; Zimmer, Andreas; Zimprich, Annemarie; Holmes, Chris; Steel, Karen P.; Herault, Yann; Gailus-Durner, Valerie; Mallon, Ann-Marie; Brown, Steve D. M. 分享 收藏
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity Joyce, Peter I.; Mcgoldrick, Philip; Saccon, Rachele A.; Weber, William; Fratta, Pietro; West, Steven J.; Zhu, Ning; Carter, Sarah; Phatak, Vinaya; Stewart, Michelle; Simon, Michelle; Kumar, Saumya; Heise, Ines; Bros-Facer, Virginie; Dick, James; Corrochano, Silvia; Stanford, Macdonnell J.; Tu Vinh Luong; Nolan, Patrick M.; Meyer, Timothy; Brandner, Sebastian; Bennett, David L. H.; Ozdinler, P. Hande; Greensmith, Linda; Fisher, Elizabeth M. C.; Acevedo-Arozena, Abraham 分享 收藏
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features Tucci, Valter; Kleefstra, Tjitske; Hardy, Andrea; Heise, Ines; Maggi, Silvia; Willemsen, Marjolein H.; Hilton, Helen; Esapa, Chris; Simon, Michelle; Buenavista, Maria-Teresa; McGuffin, Liam J.; Vizor, Lucie; Dodero, Luca; Tsafitaris, Sotirios; Romero, Rosario; Nillesen, Willy N.; Vissers, Lisenka E. L. M.; Kempers, Marlies J.; Vulto-van Silfhout, Anneke T.; Iqbal, Zafar; Orlando, Marta; Maccione, Alessandro; Lassi, Glenda; Farisello, Pasqualina; Contestabile, Andrea; Tinarelli, Federico; Nieus, Thierry; Raimondi, Andrea; Greco, Barbara; Cantatore, Daniela; Gasparini, Laura; Berdondini, Luca; Bifone, Angelo; Gozzi, Alessandro; Wells, Sara; Nolan, Patrick M. 分享 收藏
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb Kurapati, Ramakrishna; McKenna, Caoimhe; Lindqvist, Johan; Williams, Debbie; Simon, Michelle; LeProust, Emily; Baker, Jane; Cheeseman, Michael; Carroll, Natalie; Denny, Paul; Laval, Steve; Lochmueller, Hanns; Ochala, Julien; Blanco, Gonzalo 分享 收藏
Pkd1l1 establishes left-right asymmetry and physically interacts with Pkd2 Field, Sarah; Riley, Kerry-Lyn; Grimes, Daniel T.; Hilton, Helen; Simon, Michelle; Powles-Glover, Nicola; Siggers, Pam; Bogani, Debora; Greenfield, Andy; Norris, Dominic P. 分享 收藏
Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1 Baker, Jane; Riley, Genna; Romero, M. Rosario; Haynes, Andrew R.; Hilton, Helen; Simon, Michelle; Hancock, John; Tateossian, Hilda; Ripoll, Vera M.; Blanco, Gonzalo 分享 收藏
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